Allele Registry

Canonical Allele Identifier: PA106829

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.7764214087

Score -1.109334997

Score -0.9849378072

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000131726

RCV000475086

RCV000785479

RCV001310211

RCV001781474

RCV003467184

ClinVar Variation:

142536

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Arg337Cys	CA000010 NM_000546.6:c.1009C>T